Quality control & lab testing
In-house laboratory and third-party verification. Nothing enters production, and nothing leaves it, without documentation.

Service overview
Quality control & lab testing
Quality control is the part of manufacturing nobody asks about until something goes wrong, and by then the answer costs a recall instead of a test. We built the system the other way around. No raw material enters our production without a technical data sheet and a certificate of analysis, and no batch leaves without documentation that stands up on its own.
Control runs at three points rather than one. Incoming materials are checked against specification before they are released to production. In-process control monitors weight, homogeneity, fill and seal integrity while the batch is running, because a deviation caught on the line is a correction and a deviation caught afterwards is a write-off. Finished batches are verified against the specification you signed, and where the product calls for it we send samples to accredited external laboratories for independent confirmation.
We were the first supplement manufacturer in Slovenia to hold GMP certification, and the system underneath it is audited rather than declared. ISO 9001:2015 covers the process discipline, recognised internationally through IQNet, alongside SIQ and IFS Food for working with food and supplements. What that gives you in practice is retrievability. When a retailer, an authority or your own regulatory team asks about a batch made four years ago, the record exists and we can find it.
Capabilities & Features
Product assembly
Category
Details
What we test
Identity and specification of incoming raw materials
Active content and assay verification
Microbiological and heavy metal screening
Weight, fill accuracy and blend homogeneity
Seal integrity and packaging conformity
How control is organised
In-house laboratory for routine and release testing
Accredited third-party laboratories for independent confirmation
Retained reference samples from every batch
Stability testing supporting your declared shelf life
Deviation handling and documented corrective action
What you receive
Certificate of analysis for every batch
Full batch record and production documentation
Traceability from finished unit back to supplier lot
Specification and TDS for the finished product
Documentation ready for audits, listings and regulatory files

Simple & Transparent
How a project runs
Step 1
Formula and feasibility
Step 2
Sample and specification
Step 3
Production and paperwork
Common questions
Frequently asked questions
Get in touch
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